Evidence map›Paper›PMID 36036827›Full record

ArticleJournal, genetic engineering & biotechnology2022

Impact of rs11024102 PLEKHA7, rs3753841 COL11A1 single nucleotide polymorphisms, and serum levels of oxidative stress markers on the risk of primary angle-closure glaucoma in Egyptians.

Marwa Aswa, Hazem Helmy, Shahira Noweir, Somaia Ismail, AlShaimaa Taha, Azza Atef

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Article in Journal, genetic engineering & biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Marwa AswaDepartment of Biochemistry, Faculty of Science, Ain Shams University, Abbassia, Cairo, 11566, Egypt.
Hazem HelmyDepartment of Glaucoma and Optic Nerve Disease, Research Institute of Ophthalmology, Giza, Egypt.
Shahira NoweirDepartment of Human Genetics, Research Institute of Ophthalmology, Giza, Egypt.
Somaia IsmailDepartment of Medical Molecular Genetics, Division of Human Genetics and Genome Research, National Research Center, Giza, Egypt.
AlShaimaa TahaDepartment of Biochemistry, Faculty of Science, Ain Shams University, Abbassia, Cairo, 11566, Egypt. alshaimaa.taha@sci.asu.edu.eg.ORCID http://orcid.org/0000-0002-6825-466X
Azza AtefDepartment of Biochemistry, Faculty of Science, Ain Shams University, Abbassia, Cairo, 11566, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrimary angle-closure glaucoma (PACG) is one of the major causes of blindness in the Middle East with genetic loci and systemic oxidative stress as potential risk factors. The current case-control study aimed to investigate the associations of rs11024102 in Pleckstrin homology domain-containing family A member 7 (PLEKHA7), rs3753841 in collagen 11 A1 (COL11A1), and the systemic oxidative stress markers with PACG in Egyptian patients. Thirty-five control subjects and 64 PACG patients were enrolled in this study. The polymorphisms in PLEKHA7 and COL11A1 were analyzed using quantitative PCR, and their associations were statistically tested with PACG at homozygous, heterozygous, dominant, and recessive genetic models. The levels of malondialdehyde (MDA), advanced glycation-end product (AOPP), protein carbonyl (PC), and ischemia modified albumin (IMA) were quantitated colorimetrically, and their associations with PACG were analyzed statistically. The associations of MDA, AOPP, PC, and IMA with elevated intraocular pressure (IOP) were statistically tested.

resultsNeither significant difference in the genotype distribution nor allele frequency of PLEKHA7 11024102 T>C (p = 0.425 and 0.517, respectively) and COL11A1 rs3753841 G>A (p = 0.600 and 0.473, respectively) were recorded under any of the tested genetic models. Either rs11024102 PLEKHA7 or rs3753841 COL11A1 was not significantly (p > 0.025 after Bonferroni correction) associated with an increased risk of PACG in Egyptians. Egyptian patients with PACG showed significant elevations in the serum levels of MDA, AOPP, and PC either in patients with or without cases with diabetes mellites, hypertension, coronary vascular diseases, and smoking. Serum levels of MDA, AOPP, and PC were significantly associated with PACG in Egyptians (p < 0.013 after Bonferroni correction). However, MDA and PC only showed significant associations with the elevation in the IOP (p = 0.007 and 0.045, respectively) in PACG patients.

conclusionBoth rs11024102 and rs3753841 could not be considered as potential gene-dependent risk factors for PACG pathogenesis in Egyptians. On the other hand, serum levels of MDA, AOPP, and PC might be considered risk factors for PACG. Moreover, MDA and PC could serve as good predictors for the elevation of the IOP in PACG disease.

Indexed as

Advanced glycation-end productAssociationIntraocular pressureMalondialdehydePolymorphismPredictorsProtein carbonylRisk factors

Identifiers

PMID36036827
PMCPMC9424413

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